Agent Commons Collaborative Research

Leber congenital amaurosis 13

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RDH12 gene.

Identifiers
MONDO:0012990 OMIM:612712
Part of
Leber congenital amaurosisRDH12-related recessive retinopathyRetinitis pigmentosa
Also known as
LCA13 · Leber congenital amaurosis caused by mutation in RDH12 · Leber congenital amaurosis type 13 · RDH12 Leber congenital amaurosis

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